Composition of matter comprising of the creation of a low molecular weight hydrocarbon fluid exhibiting oligomerized pentenes mainly comprised of 2-Methyl-2-Butene subunits as well as related plant isoprenoids composed of 2-Methyl-1-Butene subunits and other hydrocarbons from hydrocarbon-bearing woody biomass and a process for the extraction and refinement in making the same composition through the creation of solvent permeable woody biomass particles and a multi-phase solvent extraction

ABSTRACT

A composition of matter with of the creation of a low molecular weight hydrocarbon fluid called Wood Phytoleum from woody Pinaceae and Myrtaceae biomass and a process for the extraction and refinement in making the same composition of matter through the reduction of the particle size of the raw woody biomass to form a solvent permeable particle and a phased multi-wash solvent system of extraction and refinement. A preferred embodiment includes the steps of the reduction of the particle size of the raw woody biomass to form a solvent permeable particle by shearing and chipping, the application of a phased multi-wash solvent system to the solvent permeable particle utilizing a non-polar solvent together with a bridge solvent soluble in both the non-polar solvent and in water, the application of a final bridge solvent wash to the solvent permeable particle, a mechanism for washing the particles of the woody biomass within the multi-wash solvent system, a mechanism for the collection of the solvent and Wood Phytoleum solution from the multi-wash solvent system, the extraction of the solvent from the solvent saturated particles of the woody biomass and the discharge for continued use of the woody biomass, and a process and mechanism for the extraction, collection and refinement of the solvent and Wood Phytoleum solution to discharge the solvents for reuse and to collect the Wood Phytoleum liquid oil including Pinene A and Pinene B and other oligomerized pentenes.

A composition of matter comprising of the creation of a low molecular weight hydrocarbon fluid exhibiting oligomerized pentenes mainly comprised of 2-Methyl-2-Butene subunits as well as related plant isoprenoids composed of 2-Methyl-1-Butene subunits and other hydrocarbons from hydrocarbon-bearing woody biomass and a process for the extraction and refinement in making the same composition through the creation of solvent permeable woody biomass particles and a multi-phase solvent extraction.

CROSS REFERENCE TO RELATED APPLICATIONS

This is a continuation in part of Ser. No. 12/931,433, filed on Feb. 1, 2011.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

Not Applicable

DESCRIPTION OF ATTACHED APPENDIX

Not Applicable

BACKGROUND OF THE INVENTION

This invention relates generally to the field of petroleum and more specifically to a composition of matter comprising of the creation of a low molecular weight hydrocarbon fluid exhibiting oligomerized pentenes mainly comprised of 2-Methyl-2-Butene subunits as well as related plant isoprenoids composed of 2-Methyl-1-Butene subunits and other hydrocarbons from hydrocarbon-bearing woody biomass and process for the extraction and refinement in making the same composition through the creation of solvent permeable woody biomass particles and a multi-phase solvent extraction.

This invention relates generally to the field of the manufacture of plant hydrocarbon called Phytoleum, and more specifically to a composition of matter comprising of the creation of a low molecular weight hydrocarbon fluid exhibiting mainly oligomerized pentenes mainly comprised of 2-Methyl-2-Butene subunits as well as related plant isoprenoids composed of other isoprene derived 2-Methyl-1-Butene subunits and other hydrocarbons from woody biomass and a process for the extraction and refinement in making the same composition through the creation of solvent permeable particle and a multi-phase solvent extraction methodology.

Hydrocarbons are the source of many fuel and chemical feedstocks used for industry and commerce in the world. Petroleum is the predominant source of these hydrocarbons. This petroleum is sourced from geological deposits located beneath the earth. These hydrocarbons are then refined and reformed and used as source chemicals for fuels and feedstocks. Traditionally these hydrocarbons are sourced from geological resources, however, hydrocarbons can be found in most living organisms. As hydrocarbons are produced by living organisms, these organisms can be cultivated and processed for use as source hydrocarbons. The ideal organisms for use as petroleum substitutes use the power of the Sun to fully reduce carbon dioxide into source hydrocarbons.

Higher plants produce hydrocarbon compounds composed primarily of isoprenoids. These are often in the form of terpenes made from pentene subunits. Most plants produce these isoprenoid terpenes in small amounts and utilize them to form more complex biochemicals. But some plants produce terpenes as a major metabolic product that can form a plurality of total dry biomass. A prominent example is Euphorbia tirucalli. The biochemicals in this species are very low in molecular weight and are mainly hydrocarbon. Plants that isolate and concentrate large amounts of hydrocarbons can be found often in the Pinaceae, Myrtaceae, Styracaceae, Burseraceae and Euphorbiaceae families. These are more commonly known as the pine, myrtle, styrax and spurge families. Pines from antiquity to early modern times had their hydrocarbons used as tar for naval stores, or turpentine for cleaning solvents. Myrtles generally yield more oxygenated and pleasant smelling hydrocarbons that are used in cough drops and vapor rubs containing Eucalyptus. Styraxes and myrrhs have been associated with resinous perfumes and incense since Biblical times. Spurges are so named because their hydrocarbon products are often poisonous and cause the body to purge itself of “toxins” that were thought to cause disease before the discovery of bacteria.

Some members of the family Euphorbiaceae, Pinaceae, and Myrtlaceae in particular have very high levels of hydrocarbon present within tissues. Higher plants, such as pines, produce hydrocarbons primarily from isoprene derived pentenes, 2-Methyl-2-Butene, and 2-Methyl-1-Butene. These pentenes are then constructed via cellular metabolism into other chemicals such as hormones, energy stores, or defense chemicals. Another unique isoprene derived class of molecules are rubbers. Rubbers are diene polymers composed of long poly-isoprene chains and can have a wide range of molecular weights depending on the number of isoprene monomers. Wood Phytoleum has a relatively low molecular weight group of oligomerized pentene metabolites, made of a few monomers, and the invention actually facilitates and selects for lower molecular weight hydrocarbons via solvent action. Woody hydrocarbon bearing plants that produce large amounts of liquid terpenes are ideal for use in this invention. This invention focuses on woody biomass chips as the preferred material for use in this invention with particular attention to Pinaceae and Myrtaceae species due to their availability and use in existing pulp and paper industries.

Attempts in the prior art have focused on enzyme and pyrolysis based assistance in breaking down the wood biomass to convert its energy into two main classes of fuel feedstocks, cellulosic ethanol or bio-crudes. Cellulosic ethanol has been derived from wood by breaking the cellulosic material down into simple sugars to be fermented by yeast or bacteria into ethanol. Bio-crudes have largely been produced by pyrolyzing the material and breaking lignin and cellulose to smaller molecules. Bio-crudes generally have a very high oxygen content for a petroleum substitute due to the high oxygen content of cellulose and lignin in the wood biomass itself. The prior art suffered from inefficiencies due to the energy costs required to achieve pyrolysis, The complexities of breaking down the wood material enzymatically, and the costs to derive the enzymes and provide an optimal environment required for processing the biomass into a fuel feedstock. Also the utilization of the fuel feedstocks has been less than smooth, as they are significant chemical differences between them and petroleum derived fuel feedstocks. Converting wood into ethanol, or bio-crude is a generally inefficient process, and it destroys and consumes the wood leaving little to no potential aftermarket for the processed biomass. The novelty of this invention is that it produces a chemically superior fuel feedstock to the prior art, as well as leaving the biomass in a form suitable for aftermarket use in pulp and paper production, pelletization, or chipboard manufacture.

The use of plant hydrocarbons is not new, but a novelty of this invention deals with a process isolating and selecting for petroleum-like hydrocarbons from hydrocarbon bearing woody plant material for the creation of a composition of matter to be used as a petroleum substitute. The nature of this invention includes a process for preparing and executing a low temperature solvent extraction of plant hydrocarbon. This invention develops a simpler and more economic way of yielding a composition of matter suitable as a petroleum substitute, Wood Phytoleum, from plant biomass in a continuous process focusing on Pinaceae and Myrtaceae biomass as the preferred feedstock for use. Prior technologies intended to derive fuel from woody biomass have focused on enzymatic and pyrolysis based applications to derive bio-crudes or cellulosic ethanol. The prior arts suffer from inefficiencies in economy and output and product quality.

BRIEF SUMMARY OF THE INVENTION

The primary object of the invention is to provide for the creation of a new hydrocarbon fuel source called Wood Phytoleum.

Another object of the invention is to provide for the creation of a new hydrocarbon fuel source that is carbon neutral.

Another object of the invention is to provide for the creation of a hydrocarbon fluid fuel source that is compatible with existing means of distribution and augmentation of existing petroleum-based fuels.

A further object of the invention is to provide for the creation of a plant based source for hydrocarbon fluid fuel that is sufficiently high yielding to be economically viable.

Yet another object of the invention is to provide a process for the efficient extraction and refinement of naturally occurring hydrocarbon elements in plant based organic material.

Still yet another object of the invention is to provide a process for the utilization of solvents in the extraction and refinement of naturally occurring hydrocarbon elements in plant based organic material.

Another object of the invention is to provide a process for the utilization of solvents in the extraction and refinement of naturally occurring hydrocarbon elements in plant based organic material.

Another object of the invention is to identify Pinaceae and Myrtaceae biomass in the process of the extraction and refinement of a new hydrocarbon fluid fuel source.

A further object of the invention is to provide a process that utilizes Pinaceae and Myrtaceae biomass such that the biomass retains its intended utility.

Yet another object of the invention is to provide a process that increases the utility and efficient use of Pinaceae and Myrtaceae biomass from its current uses.

Other objects and advantages of the present invention will become apparent from the following descriptions, taken in connection with the accompanying drawings, wherein, by way of illustration and example, an embodiment of the present invention is disclosed.

In accordance with a preferred embodiment of the invention, there is disclosed the creation of a composition of matter comprising of a low molecular weight hydrocarbon fluid exhibiting oligomerized pentenes mainly comprised of 2-Methyl-2-Butene subunits as well as related plant isoprenoids composed of 2-Methyl-1-Butene subunits and other hydrocarbons from hydrocarbon-bearing woody biomass and a process for the extraction and refinement in making the same composition of matter through the utilization of woody Pinaceae and Myrtaceae biomass, the reduction of the particle size of the woody Pinaceae and Myrtaceae biomass by chipping or cleaving, the formation of a solvent permeable particle from the woody Pinaceae and Myrtaceae biomass, the application of a phased multi-wash solvent system to the solvent permeable particle of the woody Pinaceae and Myrtaceae biomass, the utilization of two types of solvents in the multi-wash solvent system, the utilization of a non-polar solvent such as hexane together with a bridge solvent soluble in both the non-polar solvent and in water, a mechanism for washing the particles of the woody Pinaceae and Myrtaceae biomass within the multi-wash solvent system, the collection of the solvent and Wood Phytoleum solution from the multi-wash solvent system, the extraction of the solvent from the particles of the woody Pinaceae and Myrtaceae biomass and the discharge for use of the woody biomass, and the extraction and refinement by centrifuge and distillation and other methods of the solvent and Wood Phytoleum solution.

In accordance with a preferred embodiment of the invention, there is disclosed a process for producing Wood Phytoleum—a composition of matter comprising of the creation of a low molecular weight hydrocarbon fluid exhibiting oligomerized pentenes mainly comprised of 2-Methyl-2-Butene subunits as well as related plant isoprenoids composed of 2-Methyl-1-Butene subunits and other hydrocarbons—from hydrocarbon-bearing woody biomass through the utilization of woody Pinaceae and Myrtaceae biomass, the reduction of the particle size of the woody Pinaceae and Myrtaceae biomass by chipping or cleaving, the formation of a solvent permeable particle from the woody Pinaceae and Myrtaceae biomass, the application of a phased multi-wash solvent system to the solvent permeable particle of the woody Pinaceae and Myrtaceae biomass, the utilization of two types of solvents in the multi-wash solvent system, the utilization of a non-polar solvent such as hexane together with a bridge solvent soluble in both the non-polar solvent and in water, a mechanism for washing the particles of the woody Pinaceae and Myrtaceae biomass within the multi-wash solvent system, the collection of the solvent and Wood Phytoleum solution from the multi-wash solvent system, the extraction of the solvent from the particles of the woody Pinaceae and Myrtaceae biomass and the discharge for use of the woody biomass, and the extraction and refinement by centrifuge and distillation and other methods of the solvent and Wood Phytoleum solution.

BRIEF DESCRIPTION OF THE DRAWINGS

The drawings constitute a part of this specification and include exemplary embodiments to the invention, which may be embodied in various forms. It is to be understood that in some instances various aspects of the invention may be shown exaggerated or enlarged to facilitate an understanding of the invention.

FIG. 1 is a depiction of Pinaceae; Pinus taeda biomass.

FIG. 2 is a depiction of Myrtaceae; Eucalyptus globulus biomass.

FIG. 3 is a high-level flow chart schematic diagram of the overall process of converting raw woody biomass into Wood Phytoleum, water, water solubles, and de-oiled wood particles.

FIG. 4 Part 1 is an illustrated block diagram of the initial biomass handling in the woody particle creation process; consisting of FIG. 4, Part 1 (A) and 1 (B).

FIG. 4, Part 1(A) is a depiction of raw woody biomass entering the process chain.

FIG. 4, Part 1(B) is a depiction of a Chain Flail Delimbing and Debarking the biomass.

FIG. 4 Part 2 is an illustrated block diagram of the debarked and delimbed longwood handling; consisting of FIG. 4, Part 2 (C), 2 (D), and 2 (E).

FIG. 4, Part 2(C) is a depiction of debarked and delimbed longwood logs.

FIG. 4, Part 2(D) is a depiction of a sideview cutaway of a commercial drum chipper applying shearing and compressive forces to longwood logs.

FIG. 4, Part 2(E) is a depiction of woody particles derived from longwood suitable for Wood Phytoleum production, then subsequently pulp and paper production.

FIG. 4 Part 3 is a illustrated block diagram of the Limb, bark, and leafy biomass handling; consisting of FIG. 4, Part 3 (F), 3 (G), and 3 (H).

FIG. 4, Part 3(F) is a depiction of limbs, bark, and leaves.

FIG. 4, Part 3(G) is a depiction of a sideview cutaway of a commercial drum chipper applying shearing and compressive forces to the biomass.

FIG. 4, Part 3(H) is a depiction of woody particles derived from limbs, bark, and leaves suitable for Wood Phytoleum production, then subsequently for aftermarket uses.

FIG. 5 is a depiction of common solvent chemicals suitable for use in this invention.

FIG. 6 is a high level schematic representation of a solvent multiphase wash system.

FIG. 6 includes an ellipsis representing any number of repeated wash cycles between the first and final series of washes.

FIG. 6 includes the final wash with bridge solvent to purge the wood particle of Wood Phytoleum solvent mixture.

FIG. 7 is a high level schematic of a solvent recovery unit.

FIG. 8 is a illustrated block diagram of the liquid fraction handling and lipophillic and hydrophilic fraction separation, consisting of FIG. 8, Parts (A), (B), and (C):

FIG. 8 (A) includes a depiction of a liquid fraction collection holding tank.

FIG. 8 (B) includes a depiction of a clarifying process to remove contaminants.

FIG. 8 (C) includes a depiction of a centrifuge unit separating lipophilic and hydrophilic fractions.

FIG. 9 is a high-level schematic of a simple distillation and solvent recovery unit.

FIG. 10 is a depiction of the major chemical building blocks found in Wood Phytoleum.

FIG. 11 is a depiction of some chemicals found in the Wood Phytoleum naphtha fraction; Heptane, Alpha Pinene, and Beta Pinene

FIG. 12 is a depiction of some chemicals found in the Wood Phytoleum grease fraction; farnesene, phytane, and squalene.

FIG. 13 is a depiction of example chemicals found in the Wood Phytoleum tar fraction; consisting of Parts 1 and 2.

FIG. 13 Part 1 is a depiction of chlorophyll a.

FIG. 13 part 2 is a depiction of beta carotene and lupenone.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

Detailed descriptions of the preferred embodiment are provided herein. It is to be understood, however, that the present invention may be embodied in various forms. Therefore, specific details disclosed herein are not to be interpreted as limiting, but rather as a basis for the claims and as a representative basis for teaching one skilled in the art to employ the present invention in virtually any appropriately detailed system, structure or manner.

The invention relates to a process by which a composition of matter being a liquid hydrocarbon mixture is extracted from woody biomass via the particle size reduction of said biomass then a multiple phased solvent wash and recovery is employed to purify the material and recover the solvent from the plant hydrocarbon. The composition of matter yielded as a hydrocarbon material is suitable for use as a fuel or chemical feedstock.

A schematic representation of the overall process is shown in FIG. 3.

The first step in the process is the formation of a solvent permeable particle from the fresh woody biomass (see FIG. 4) which will allow for efficient flow of solvent through the material to remove hydrocarbon oils. FIG. 4 depicts steps to create a solvent permeable particle, though it is not the only method by which a wood particle could be created. The process begins with the whole tree being harvested from the forest (FIG. 4 Part 1 (A)). Once harvested, it is common in the forestry industry to delimb and debark whole trees. This is because bark and leaves, and small branches are not suitable for paper production. Delimbing and debarking is often done with a chain flail (FIG. 4 Part 1 (B)). The bark, leaves, and limbs are separated from the clean logs called “longwood”, (FIG. 4 Part 3 (F)) and (FIG. 4 Part 2 (C)) respectively. These two streams are kept separate but particles created from them are equally suitable for solvent wash processing. They would ideally be kept in separate bins during washing and chip handling to maintain their final end use, paper production/chip board manufacture for the longwood particles, and burning for the bark and leaf containing particles. The longwood would be subjected to compressive and shearing forces, such as those in a drum chipper, (FIG. 4 Part 2 (D)), resulting in the creation of a solvent permeable woody particle (FIG. 4 Part 2 (E)). In the same manner the bark, limbs, and leaves (FIG. 4 Part 3 (F)) could be subjected to similar compressive and shearing forces (FIG. 4 Part 3 (G)) to create solvent permeable particles (FIG. 4 Part 3 (H)). The overall goal of woody particle creation is particle size reduction and this is achieved by applying compressive and shearing forces to the biomass to create a material that is conducive and efficient for solvent flow and extraction. The preferred methodology would cleave the woody biomass along the vascular tissue comprising the grain of the wood. The intention of this invention is to utilize commercially available drum or disk wood chipping equipment to achieve this task. As opposed to herbaceous hydrocarbon bearing biomass processing, woody biomass will be less pulverized and have a larger average particle size. However smaller “sawdust” sized particles such as those for use in wood pelletization are also suitable for this invention. As opposed to herbaceous biomass processing for Phytoleum, there will not be any production of a bat. The wood particle is the sole product of this process and is not limited in its source of production. FIG. 4 simply provides background as to how a real world application would create a wood particle suitable for this invention. After the particle is produced it is ready for de-oiling in a multiphased solvent wash setup.

The next step is to subject the woody material to a phased multi-wash solvent system. Due to the larger particle sizes of processed woody biomass, solvent dynamics are more important than in the processing of herbaceous hydrocarbon bearing biomass. As opposed to processing of herbaceous material such as Euphorbia tirucalli, woody material requires the action of at least two types of solvents. One solvent needs to be non-polar and the solvent of preferable use in the methodology is hexane, however other non-polar solvent solutions can be used in this process. The other solvent that is used must be a solvent that is soluble in both water and hexane, this is called the “bridge” solvent. The solvent should also have a boiling point below that of water and be free from high percentage water azeotropes in which large portions of the water will be distilled along with the solvent. This is important in order to avoid high heat consumption per unit material arising from the phase change of water. Examples of useable solvents that fit this definition are acetone or ethanol. This water and hexane soluble “bridge” solvent is necessary in order to facilitate hexane sorption into the wood chip. The bridge solvent allows for the hexane to penetrate pockets of water in the vascular tissue to absorb the Wood Phytoleum. A good bridge solvent such as acetone or ethanol also form a depressed boiling point azeotrope. This can be utilized to further reduce energy requirements for later solvent distillation. If a bridge solvent was not utilized, the wood particle would need to be reduced further in order for the hexane to penetrate, requiring more processing and limiting aftermarket applications. Larger particles or otherwise less permeable wood particles may also benefit from elevated pressure during solvent soaking. A depiction of common solvents that can be used is in FIG. 5.

The multi phase wash system is defined by a continuous system of washing solvent through the material to where a gradient of solvent/oil mixture is achieved. The preferable method would be to use gravity, however other systems using pressure and mechanical forces could be used to achieve a similar effect. Though pressure systems for penetration will also require the addition of a blower chamber as the material is returned to ambient pressure conditions. Rotary or belt extraction processes would work well to achieve the continuous washing effect, as well as facilitate different solvent mixtures coming into contact with the chips. The solvent/oil gradient is crucial to this aspect of the invention as this allows for the most economical level of solvent to be used to extract the oil. This correlates with lower volumes of solvent needed to extract the hydrocarbon oil to minimize solvent loss and decrease the per unit energy needed to recover the solvent after extraction. The schematic representation of the overall unit is shown in FIG. 6.

Once the solvent has flowed through the material it is collected at the loading end of the unit as washer outflow in order to achieve a counter current flow of the solvent. The exact number of washes depends on the throughput and the exact plant material and solvent particle involved. However, in woody biomass processing the last wash cycle on the particle material should be a pure bridge solvent wash. This will push out any remaining lipophilic solvent/Wood Phytoleum mixture and replace it with the bridge solvent. This is done in lieu of expectoration as in herbaceous material washing as the woody particles cannot be mechanically compressed to remove the remaining Wood Phytoleum carrying solvent. Though systems including negative pressure treatment to remove the solvent could achieve a similar effect albeit with increased mechanical complexity. The schematic representation of the overall unit is shown in FIG. 6 indicating the final wash with bridge solvent only.

After the particles have transited though all solvent wash units, they would move to a solvent recovery unit to recover the solvent remaining in the particles for collection and reuse. The wood particles would be heated to drive off solvent until the levels remaining in the wood particles are suitable for system discharge.

In this manner, the de-oiled wood particles would be brought into an evaporator/boiler chamber as shown in FIG. 7. The remains of the solvent would be driven off from the wood particles using heat with or without negative pressure. This is done to recover solvent for economical processing, as well as reduce waste chemical discharge to the environment to levels compliant with governmental regulations. The size and operating conditions of the unit would correspond to throughput and the levels and type of solvent remaining in the woody particles depending on substrate.

The solution decanted from the washer units will consist of a mixture of water, water solubles, including some bridge solvent, and a solvent/Wood Phytoleum mixture. This stream of liquids and solubles would be subjected to a clarification/filtration process to remove any dirt or foreign objects that may still be in the liquids from the washer units. This can be done via a clarification process or simple filtration if the volume of liquids processed is low. Water and oil solubles need to be separated from the stream and this is best achieved via centrifugation. The schematic representations for these steps for separation of the oils and water are shown in FIG. 8 although other separation schemes such as a gravity driven separation system could be utilized, albeit more slowly. To yield a continuous system, an array of centrifuges would be employed. In this manner, the liquid phase mixture is brought into a centrifugal array. The mixture to be centrifuged exists in two phases—One lipophilic—the solvent/Wood Phytoleum solution, and one hydrophilic—the water and water solubles. After centrifugation, the solvent/Wood Phytoleum oil mixture would head to an evaporator or distillation column to remove the solvent as shown in FIG. 9. The solvent could be recovered and reused. The mixed solution of Wood Phytoleum and solvent are brought to a boil, where the solvent is being removed from the solution. This can be achieved at fairly low temperatures of about 70 to 80 degrees Celsius for hexane and pressures at around 1 atmosphere while most other non-polar solvents will require 80 to 90 degrees Celsius at around 1 atmosphere. When the a bridge solvent is included, the operating temperatures are decreased further due to positive azeotropic interaction. In some cases around 40-50 degrees Celsius. This decreases the necessary complexity of the system and lowers energy inputs, which would translate to lower costs and ease of adoption of the technology. Alternative methodologies utilize different pressure and temperature combinations which would also result in the removal of solvent including vacuum distillation. The simple distillation schematic as shown in FIG. 9 could then be followed by a fractional distillation to further process and refine the resulting Wood Phytoleum into its constituent fractions.

The Wood Phytoleum itself has fairly unique characteristics compared to vegetable oils, fats, and other more well known lipophilic biological derivatives. In particular the Pinaceae derived Wood Phytoleum is comprised of terpenes, chlorophyll, carotenes, as well as some other until now less defined and less well known materials. These metabolites which make up a plurality of the Wood Phytoleum are primarily of oligomerized pentenes. These metabolites that comprise the Wood Phytoleum oil have large portions of 2-Methyl-2-Butene and 2-methyl-1-butene subunits. These are low molecular weight hydrocarbons with very desirable properties for the petroleum industry. They are sometimes manufactured as gasoline additives and plastic polymer precursors. They can be directly distilled and utilized as a fuel or in combination with the other Wood Phytoleum constituents be refined into a suite of light petrochemical products. The Building Blocks of the composition are shown in FIG. 10 and are comprised of Isoprene, 2-Methyl-2-Butene, and 2-Methyl-1-Butene.

In the preferred exercise of the invention the process yields a composition of matter, Wood Phytoleum (see FIG. 11, FIG. 12, FIG. 13, Part 1, and FIG. 13, Part 2), of which the bulk is biologically synthesized from pentenes such that the number of carbons in Wood Phytoleum chemicals is almost always a multiple of five. In Euphorbia tirucalli derived Phytoleum the number of carbons is also usually a multiple of ten. In Pinaceae or Myrtaceae derived Wood Phytoleums this is not always the case as odd numbered hydrocarbons are just as common. Given that the number of carbons in a molecule is usually one of the greatest factors determining hydrocarbon characteristics, and that pentene derived hydrocarbons are usually only liquid up to C30, the Wood Phytoleum can be separated after extraction into three distinct fractions; naphtha, grease, and tar (see FIG. 11, FIG. 12, FIG. 13, Part 1, and FIG. 13, Part 2). Though as opposed to Phytoleum derived from Euphorbia tirucalli, the fraction boundaries of Wood Phytoleum are less well defined due to the higher presence of odd numbered carbon compounds. Also woody biomass derived Wood Phytoleum generally has a higher ratio of alpha alkenes to beta alkenes than Euphorbia tirucalli derived Phytoleum.

The lightest and ideally most abundant fraction is the Wood Phytoleum naphtha fraction (C10, rarer C5) as shown in FIG. 11. This is a clear to pale yellow liquid with a high vapor pressure and a boiling point from 30 to 200 degrees Celsius exhibiting a boiling point of mainly 150 to 160 degrees Celsius. The naptha fraction is comprised mainly of pinenes, Alpha pinene and Beta pinene, and heptane with lower concentrations of other monoterpenes such as limonenes or tirucallenes, as shown in FIG. 11. Pinenes are cyclical monoterpenes that comprise turpentine. Some species of woody plants will also generate heptane. This C7 compound (heptane) will fall into the naphtha fraction as well and will boil around 100 C if present. The second fraction is a Wood Phytoleum grease (C20, mainly C30, rarer C15, C25) as shown in FIG. 12. This is a light to golden brown liquid comprised mainly of squalene with lesser concentrations of farnesene, geranylgeranene and the related phytanes. This fraction will also hold any diterpenes that may be present in the Wood Phytoleum. The third fraction is a Wood Phytoleum tar (C35 and up, some C30) some examples of which are shown in FIG. 13, Part 1 and in FIG. 13, Part 2. This fraction holds all the solid and semisolid hydrocarbons and is usually dark green due to the presence of chlorophyll. This fraction is comprised of rubbers, carotenes, chlorophyll, and larger terpenoid molecules. Ketone groups are also present in this fraction in sterols and chlorophyll itself. Alcohols are present in greater amounts than with Phytoleum from Euphorbia tirucalli and the alcohols that are present tend to be smaller than alcohols found in Phytoleum from Euphorbia tirucalli.

While the invention has been described in connection with a preferred embodiment, it is not intended to limit the scope of the invention to the particular form set forth, but on the contrary, it is intended to cover such alternatives, modifications, and equivalents as may be included within the spirit and scope of the invention as defined by the appended claims. Although the present invention has been described in considerable detail with reference to certain preferred versions thereof, other versions are possible. Therefore, the spirit and scope of the appended claims should not be limited to the description of the preferred versions contained therein. Any element in a claim that does not explicitly state “means for” performing a specified function, or “step for” performing a specified function, is not to be interpreted as a “means” or “step” clause as specified in 35 U.S.C. Section 112 Paragraph 6. In particular, the use of the “step of” in the claims is not intended to invoke the provisions of 35 U.S.C. Section 112 Paragraph 6.

The reader's attention is directed to all papers and documents which are filed concurrently with this specification and which are open to public inspection with this specification, and the contents of all such papers and documents are incorporated herein by reference. All features disclosed in this specification (including any accompanying claims, abstract, and drawings) may be replaced by alternative features serving the same, equivalent or similar purpose, unless expressly stated otherwise. Unless expressly stated otherwise, each feature disclosed is one example only of a generic series of equivalent or similar features. 

1. A composition of matter comprising of the creation of a low molecular weight hydrocarbon fluid exhibiting mainly oligomerized pentenes mainly comprised of 2-Methyl-2-Butene subunits as well as related plant isoprenoids composed of 2-Methyl-1-Butene subunits and other hydrocarbons from woody biomass prepared by the steps of a process for the extraction and refinement in making the same composition of matter through the creation of a solvent permeable particle and a multi-phase solvent extraction system;
 2. A composition of matter as claimed in claim 1 further comprising the step(s) of the reduction in particle size of the raw woody biomass of Pinaceae and Myrtaceae by applying compressive and shearing forces to the raw woody biomass to create a material that is conducive and efficient for solvent flow and extraction through existing processes for chipping and shearing raw woody biomass;
 3. A composition of matter as claimed in claim 2 wherein said processed woody biomass is subjected to a phased multi-wash solvent system preferably using hexane or other non-polar solvent solutions together with a bridge solvent soluble in both the non-polar solvent and water such as acetone or ethanol for removal of hydrocarbon oil constituents;
 4. A composition of matter as claimed in claim 3 wherein said phased multi-wash solvent system is refined by a continuous system of washing solvents through the particulated woody biomass using gravity or pressurized solvent flows to achieve the most economical level of gradient of solvent/hydrocarbon oil mixture for extraction;
 5. A composition of matter as claimed in claim 4 further comprising the steps of processing the solvent saturated woody biomass through a final wash of only the bridge solvent, the solvent soluble in both the non-polar solvent and in water, such as acetone or ethanol in order to push out any remaining lipophilic solvent/Wood Phytoleum mixture in the solvent saturated woody biomass for collection of the liquid fraction solution;
 6. A composition of matter as claimed in claim 5 further comprising the steps of subjecting the liquid fraction solution extracted in the process to a clarification and filtration collection tank for removal of sediment and processing of the liquid fraction of the collected solution by means of a centrifugation system comprised of an array of centrifuges to separate and extract the Wood Phytoleum hydrocarbon oil from the other components;
 7. A composition of matter as claimed in claim 5 further comprising the steps of subjecting the treated and solvent saturated woody biomass particles to processing within an evaporator/boiler heat exchanger chamber where the remaining solvent would be driven off from the solvent saturated woody biomass particles using heat and or negative pressure for re-use and the woody biomass particles removed for reintroduction to existing end use utilization;
 8. A composition of matter as claimed in claim 6 further comprising the steps of subjecting the liquid solution extracted from the centrifugation system process to a distillation unit system for refinement of the final product composition by the application of pressure and thermal processes to remove any remaining components from the Wood Phytoleum hydrocarbon solution yielding Wood Phytoleum liquid oil including Pinene A and Pinene B and other oligomerized pentenes.
 9. A process for producing Wood Phytoleum—a composition of matter comprising of the creation of a low molecular weight hydrocarbon fluid exhibiting mainly oligomerized pentenes mainly comprised of 2-Methyl-2-Butene subunits as well as related plant isoprenoids composed of 2-Methyl-1-Butene subunits and other hydrocarbons from woody Pinaceae and Myrtaceae biomass through the process of the extraction and refinement in making the same composition through the creation of a solvent permeable woody biomass particle and a multi-phase solvent extraction system comprising the steps of:
 10. A process for producing Wood Phytoleum—a composition of matter as claimed in claim 9 further comprising the step(s) of the manufacture of a solvent permeable biomass by the reduction in particle size of the raw woody biomass of Pinaceae and Myrtaceae by applying compressive and shearing forces to the raw woody biomass to create a material that is conducive and efficient for solvent flow and extraction through existing processes for chipping and shearing raw woody biomass;
 11. A process for producing Wood Phytoleum—a composition of matter as claimed in claim 10 wherein said processed woody biomass is subjected to a phased multi-wash solvent system preferably using hexane or other non-polar solvent solutions together with a bridge solvent soluble in both the non-polar solvent and water such as acetone or ethanol for removal of hydrocarbon oil constituents;
 12. A process for producing Wood Phytoleum—a composition of matter as claimed in claim 11 wherein said phased multi-wash solvent system is refined by a continuous system of washing solvents through the particulated woody biomass using gravity or pressurized solvent flows to achieve the most economical level of gradient of solvent/hydrocarbon oil mixture for extraction;
 13. A process for producing Wood Phytoleum—a composition of matter as claimed in claim 12 further comprising the steps of processing the solvent saturated woody biomass through a final wash of only the bridge solvent, the solvent soluble in both the non-polar solvent and in water, such as acetone or ethanol in order to push out any remaining lipophilic solvent/Wood Phytoleum mixture in the solvent saturated woody biomass for collection of the liquid fraction solution;
 14. A process for producing Wood Phytoleum—a composition of matter as claimed in claim 13 further comprising the steps of subjecting the liquid fraction solution extracted in the process to a clarification and filtration collection tank for removal of sediment and processing of the liquid fraction of the collected solution by means of a centrifugation system comprised of an array of centrifuges to separate and extract the Wood Phytoleum hydrocarbon oil from the other components;
 15. A process for producing Wood Phytoleum—a composition of matter as claimed in claim 13 further comprising the steps of subjecting the treated and solvent saturated woody biomass particles to processing within an evaporator/boiler heat exchanger chamber where the remaining solvent would be driven off from the solvent saturated woody biomass particles using heat and or negative pressure for re-use and the woody biomass particles removed for reintroduction to existing end use utilization;
 16. A process for producing Wood Phytoleum—a composition of matter as claimed in claim 14 further comprising the steps of subjecting the liquid solution extracted from the centrifugation system process to a distillation unit system for refinement of the final product composition by the application of pressure and thermal processes to remove any remaining components from the Wood Phytoleum hydrocarbon solution yielding Wood Phytoleum liquid oil including Pinene A and Pinene B and other oligomerized pentenes. 